delusions Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A belief that is pathological and is held despite evidence to the contrary. (Human Phenotype Ontology, HP_0000746)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000746
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Genes

18 genes associated with the delusions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ARSA arylsulfatase A
C9ORF72 chromosome 9 open reading frame 72
CPOX coproporphyrinogen oxidase
CYP27A1 cytochrome P450, family 27, subfamily A, polypeptide 1
DISC2 disrupted in schizophrenia 2 (non-protein coding)
ECM1 extracellular matrix protein 1
EIF2B1 eukaryotic translation initiation factor 2B, subunit 1 alpha, 26kDa
EIF2B2 eukaryotic translation initiation factor 2B, subunit 2 beta, 39kDa
EIF2B3 eukaryotic translation initiation factor 2B, subunit 3 gamma, 58kDa
EIF2B4 eukaryotic translation initiation factor 2B, subunit 4 delta, 67kDa
EIF2B5 eukaryotic translation initiation factor 2B, subunit 5 epsilon, 82kDa
JPH3 junctophilin 3
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
PRNP prion protein
SNCA synuclein, alpha (non A4 component of amyloid precursor)
SNCB synuclein, beta
TBP TATA box binding protein
TBX1 T-box 1